Evaluation efficacy of oral probiotics on the clinical outcome in hospitalized patients with acute alcohol poisoning; A single-blinded RCT

Comparison of the efficacy of oral probiotics and placebo in clinical outcome of hospitalized patients with acute alcohol(methanol) poisoning; A single-blinded RCT

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210720051946N3

Enrollment

Registered

2022-05-31

Start date

2021-10-07

Completion date

Unknown

Last updated

2022-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute methanol intoxication. methanol poisoning

Interventions

Intervention 1: Intervention group:. Intervention 2: Control group:.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients with acute alcohol intoxication who are admitted in toxicology intensive care unit and their companion( legally eligible decision maker in their absence) approves the consent form for entering the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Length of Hospital Stay(LOHS). Timepoint: 7 days after beginning the treatment. Method of measurement: inpatient/discharge status of the patient.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPeyman Erfan Talab Evini

Shahid Beheshti University of Medical Sciences

peyman1346erfan@sbmu.ac.ir+98 21 5102 5000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026